US7517416B2 - Bulk-solidifying high manganese non-ferromagnetic amorphous steel alloys and related method of using and making the same - Google Patents
Bulk-solidifying high manganese non-ferromagnetic amorphous steel alloys and related method of using and making the same Download PDFInfo
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- US7517416B2 US7517416B2 US11/446,098 US44609806A US7517416B2 US 7517416 B2 US7517416 B2 US 7517416B2 US 44609806 A US44609806 A US 44609806A US 7517416 B2 US7517416 B2 US 7517416B2
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Images
Classifications
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C43/00—Alloys containing radioactive materials
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C45/00—Amorphous alloys
- C22C45/02—Amorphous alloys with iron as the major constituent
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C33/00—Making ferrous alloys
- C22C33/003—Making ferrous alloys making amorphous alloys
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22F—CHANGING THE PHYSICAL STRUCTURE OF NON-FERROUS METALS AND NON-FERROUS ALLOYS
- C22F1/00—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working
- C22F1/10—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of nickel or cobalt or alloys based thereon
Definitions
- the present invention is directed to the field of amorphous steel alloys with high manganese content and related method of using and manufacturing the same.
- Bulk-solidifying amorphous metal alloys are those alloys that can form an amorphous structure upon solidifying from the melt at a cooling rate of several hundred degrees Kelvin per second or lower. Most of the prior amorphous metal alloys based on iron are characterized by their soft-magnetic behavior, high magnetic permeability at high frequencies, and low saturated magnetostriction [1] [2]. The Curie temperatures are typically in the range of about 200-300° C. These alloys also exhibit specific strengths and Vickers hardness two to three times those of high-strength steel alloys; and in some cases, good corrosion-resistant properties have been reported. Ferrous-based metallic glasses have been mainly used for transformer, recording head, and sensor applications, although some hard magnetic applications have also been reported.
- the bulk-solidifying ferrous-based amorphous alloys are multicomponent systems that contain 50-70 atomic percent iron as the major component.
- the remaining composition combines suitable mixtures of metalloids (Group b elements) and other elements selected from cobalt, nickel, chromium, and refractory as well as lanthanide (Ln) metals [2] [3].
- These bulk-solidifying amorphous alloys can be obtained in the form of cylinder-shaped rods between one and six millimeters in diameter as well as sheets less than one millimeter in thickness [4].
- the good processability of these alloys can be attributed to the high reduced glass temperature T rg (defined as glass transition temperature T g divided by the liquidus temperature T l in K) of about 0.6 to 0.63 and large supercooled liquid region ⁇ T x (defined as crystallization temperature minus the glass transition temperature) of at least 20° C. that are measured.
- T rg glass transition temperature T g divided by the liquidus temperature T l in K
- ⁇ T x defined as crystallization temperature minus the glass transition temperature
- the present invention amorphous steel alloy suppresses the magnetism compared with conventional compositions while still achieving a high processability of the amorphous metal alloys and maintaining superior mechanical properties and good corrosion resistance properties.
- the present invention provides bulk-solidifying high manganese non-ferromagnetic amorphous steel alloys and related method of using and making articles (e.g., systems, structures, components) of the same.
- the present invention features an Fe-based non-ferromagnetic amorphous steel alloy comprised substantially or entirely of a composition represented by the formula: (Fe 1-a-b-c Mn a Cr b Mo c ) 100-d-e-f Zr d Nb e B f , wherein a, b, c, d, e, and f respectively satisfy the relations: 0.29 ⁇ a ⁇ 0.2, 0.1 ⁇ b ⁇ 0, 0.05 ⁇ c ⁇ 0, 10 ⁇ d ⁇ 2, 6 ⁇ e ⁇ 0, 24 ⁇ f ⁇ 13.
- the present invention features an Fe-based amorphous steel alloy comprised substantially of a composition represented by the formula: (Fe 1-a-b-c Mn a Cr b Mo c ) 100-d-e-f Zr d Nb e B f , wherein a, b, c, d, e, and f respectively satisfy the relations 0.29 ⁇ a ⁇ 0.2, 0.1 ⁇ b ⁇ 0, 0.05 ⁇ c ⁇ 0, 10 ⁇ d ⁇ 2, 6 ⁇ e ⁇ 0, 24 ⁇ f ⁇ 13, and wherein the alloy has a critical cooling rate of less than about 1,000° C./sec.
- the present invention features an Fe-based amorphous steel alloy comprised substantially of a composition represented by the formula: (Fe 1-a-b-c Mn a Cr b Mo c ) 100-d-e-f Zr d Nb e B f , wherein a, b, c, d, e, and f respectively satisfy the relations 0.29 ⁇ a ⁇ 0.2, 0.1 ⁇ b ⁇ 0, 0.05 ⁇ c ⁇ 0, 10 ⁇ d ⁇ 2, 6 ⁇ e ⁇ 0, 24 ⁇ f ⁇ 13, and wherein the alloy is processable into bulk amorphous sample of at least about 0.1 mm in thickness in its minimum dimension.
- the present invention features an Fe-based non-ferromagnetic amorphous steel alloy comprised substantially or entirely of a composition represented by the formula: Fe 100-a-b-c-d-e Mn a Mo b Cr c B d C e , wherein a, b, c, d, and e respectively satisfy the relations: 13 ⁇ a ⁇ 8, 17 ⁇ b ⁇ 12, 5 ⁇ c ⁇ 0, 7 ⁇ d ⁇ 4, 17 ⁇ e ⁇ 13 (these subscript values indicating the atomic percent amounts of the constituent elements of the composition).
- the present invention features an Fe-based amorphous steel alloy comprised substantially of a composition represented by the formula: Fe 100-a-b-c-d-e Mn a Mo b Cr c B d C e , wherein a, b, c, d, and e respectively satisfy the relations 13 ⁇ a ⁇ 8, 17 ⁇ b ⁇ 12, 5 ⁇ c ⁇ 0, 7 ⁇ d ⁇ 4, 17 ⁇ e ⁇ 13, these subscript values indicating the atomic percent amounts of the constituent elements of the composition; and wherein the alloy has a critical cooling rate of less than about 1,000° C./sec.
- the present invention features an Fe-based amorphous steel alloy comprised substantially of a composition represented by the formula: Fe 100-a-b-c-d-e Mn a Mo b Cr c B d C e , wherein a, b, c, d, and e respectively satisfy the relations 13 ⁇ a ⁇ 8, 17 ⁇ b ⁇ 12, 5 ⁇ c ⁇ 0, 7 ⁇ d ⁇ 4, 17 ⁇ e ⁇ 13, these subscript values indicating the atomic-percent amounts of the constituent elements of the composition; and wherein the alloy is processable into bulk amorphous sample of at least about 0.1 mm in thickness in its minimum dimension.
- the present invention features an Fe-based non-ferromagnetic amorphous steel alloy comprised substantially or entirely of a composition represented by the formula: Fe 100-a-b-c-d-e-f Mn a Mo b Cr c B d P e C f , wherein a, b, c, d, e, and f respectively satisfy the relations: 15 ⁇ a ⁇ 5, 14 ⁇ b ⁇ 8, 10 ⁇ c ⁇ 4, 8 ⁇ d ⁇ 0, 12 ⁇ e ⁇ 5, 16 ⁇ f ⁇ 4 (these subscript values indicating the atomic percent amounts of the constituent elements of the composition).
- the present invention features an Fe-based amorphous steel alloy comprised substantially of a composition having the formula: Fe 100-a-b-c-d-e-f Mn a Mo b Cr c B d P e C f , wherein a, b, c, d, e, and f respectively satisfy the relations 15 ⁇ a ⁇ 5, 14 ⁇ b ⁇ 8, 10 ⁇ c ⁇ 4, 8 ⁇ d ⁇ 0, 12 ⁇ e ⁇ 5, 16 ⁇ f ⁇ 4, these subscript values indicating the atomic percent amounts of the constituent elements of the composition; and wherein the alloy has a critical cooling rate of less than about 1,000° C./sec.
- the present invention features an Fe-based amorphous steel alloy comprised substantially of a composition having the formula: Fe 100-a-b-c-d-e-f Mn a Mo b Cr c B d P e C f , wherein a, b, c, d, e, and f respectively satisfy the relations 15 ⁇ a ⁇ 5, 14 ⁇ b ⁇ 8, 10 ⁇ c ⁇ 4, 8 ⁇ d ⁇ 0, 12 ⁇ e ⁇ 5, 16 ⁇ f ⁇ 4, these subscript values indicating the atomic percent amounts of the constituent elements of the composition; and wherein the alloy is processable into bulk amorphous sample of at least about 0.1 mm in thickness in its minimum dimension.
- the present invention features method of producing a feedstock of the Fe-based alloy comprising the steps of: (a) melting at least substantially all elemental components together of the Fe-based alloy except Mn (preferably in an arc furnace) so as to provide at least one Mn-free ingot; (b) melting at least one the Mn-free ingot together with Mn forming at least one final ingot; and (c) bulk-solidifying at least one the final ingot through conventional mold casting.
- the present invention features method of producing “homogeneously alloyed” feedstock for the Fe-based alloy, which comprises the steps: (a) melting at least substantially all elemental components together of the Fe-based alloy except Mn to provide at least one Mn-free ingot; and (b) melting at least one the Mn-free ingot together with Mn forming at least one final ingot.
- the present invention features method of producing a feedstock of the Fe-based alloy comprising the steps of: (a) melting substantially all elemental components together of the Fe-based alloy except Mn (preferably in an arc furnace) to provide at least one Mn-free ingot; (b) melting Mn obtaining at least one clean Mn; (c) melting at least one the Mn-free ingot together with at least one the clean Mn forming a final ingot; and (d) bulk-solidifying at least one the final ingot through mold casting.
- the present invention features method of producing “homogeneously alloyed” feedstock for the Fe-based alloy, which comprises the steps: (a) melting substantially all elemental components together of the Fe-based alloy except Mn to provide at least one Mn-free ingot; (b) melting Mn obtaining at least one clean Mn; and (c) melting at least one the Mn-free ingot together with at least one the clean Mn forming a final ingot.
- the present invention features method of producing the Fe-based alloy comprising the steps of: (a) mixing Fe, C, Mo, Cr, and B forming a mixture; (b) pressing the mixture into at least one mass; (c) melting at least one the mass in a suitable furnace forming at least one preliminary ingot; (d) melting at least-one the preliminary ingot with Mn to form at least one final ingot; and (e) bulk-solidifying at least one the final ingot through mold casting.
- the present invention features a method of producing “homogeneously alloyed” feedstock for the Fe-based alloy, which comprises the steps: (a) mixing Fe, C, Mo, Cr, and B forming a mixture; (b) pressing the mixture into at least one mass; (c) melting at least one the mass in a furnace forming at least one preliminary ingot; and (d) melting at least one the preliminary ingot with Mn to form at least one final ingot.
- the present invention features a method of producing the Fe-based alloy comprising the steps of: (a) mixing Fe, C, Mo, Cr, B, and P forming a mixture; (b) pressing the mixture into at least one mass; (c) melting at least one the mass in a furnace forming at least one preliminary ingot; (d) melting at least one the preliminary ingot with Mn to form at least one final ingot; and (e) bulk-solidifying at least one the final ingot through mold casting.
- the present invention features a method of producing “homogeneously alloyed” feedstock for the Fe-based alloy, which comprises the steps: (a) mixing Fe, C, Mo, Cr, B, and P forming a mixture; (b) pressing the mixture into at least one mass; (c) melting at least one the mass in a furnace forming at least one preliminary ingot; and (d) melting at least one the preliminary ingot with Mn to form at least one final ingot.
- the present invention provides both the non-ferromagnetic properties at ambient temperature as well as useful mechanical attributes.
- the present invention is a new class of ferrous-based bulk-solidifying amorphous metal alloys for non-ferromagnetic structural applications.
- the present invention alloys exhibit magnetic transition temperatures below the ambient, mechanical strengths and hardness superior to conventional steel alloys, and good corrosion resistance.
- the present invention alloys for example, contain either high manganese addition or high manganese in combination with high molybdenum and carbon additions.
- the present invention alloys exhibit high reduced glass temperatures and large supercooled liquid regions comparable to conventional processable magnetic ferrous-based bulk metallic glasses. Furthermore, since the synthesis-processing methods employed by the present invention do not involve any special materials handling procedures, they are directly adaptable to low-cost industrial processing technology.
- Metalloids tend to restore the Curie point that is otherwise suppressed by adding refractory metals to amorphous ferrous-based alloys.
- the addition of manganese is very effective in suppressing ferromagnetism [5].
- the addition of about 10 atomic percent or higher manganese content reduces the Curie point to below ambient temperatures,as measured by using a Quantum Design MPMS system.
- the Curie point and spin-glass transition temperatures are observed to be below about ⁇ 100° C.
- the present invention reveals that the addition of manganese to ferrous-based multi-component alloys is largely responsible for the high fluid viscosity observed. High fluid viscosity enhances the processability of amorphous alloys.
- compositions of the present invention reveal that when molybdenum and chromium are added they provide the alloys with high hardness and good corrosion resistance. Accordingly, the present invention alloys contain comparable or significantly higher molybdenum content than conventional steel alloys. Preliminary measurements in an embodiment of the present invention show microhardness in the range of about 1200-1600 DPN and tensile fracture strengths of at least about 3000 MPa; values that far exceed those reported for high-strength steel alloys.
- FIG. 1 illustrates an x-ray diffraction pattern from exemplary sample pieces of total mass about 1 gm obtained by crushing a 4 mm-diameter as-cast rod of the present invention MnMoC-class amorphous ferrous alloy.
- FIG. 2 illustrates a differential thermal analysis plots obtained at scanning rate of 10° C./min showing glass transition (indicated by arrows), crystallization, and melting in two present invention exemplary amorphous steel alloys of the MnB class.
- FIG. 3 illustrates differential thermal analysis plots obtained at scanning rate of 10° C./min showing glass transition (indicated by arrows), crystallization, and melting in two exemplary amorphous steel alloys of the MnMoC class. The partial trace is obtained upon cooling.
- FIG. 4 illustrates a potentiodynamic polarization trace obtained on one of the present invention exemplary MnB-class amorphous alloy sample immersed in 0.6M NaCl pH: 6.001 solution.
- FIG. 5 illustrate segments of two exemplary amorphous rods, one 3 mm (Fe 50 Mn 10 Mo 14 Cr 4 C 15 B 7 , bottom sample) in diameter and one 4 mm (Fe 52 Mn 10 Mo 14 Cr 4 C 15 B 6 , top sample) in diameter, obtained by injection casting.
- FIG. 6 illustrate a typical potentiodynamic polarization trace obtained on exemplary 3 mm-diameter samples of amorphous Fe 52 Mn 10 Mo 14 Cr 4 B 6 C 14 .
- the present invention provides a novel non-ferromagnetic glassy alloy at ambient temperature and related method of using and making articles (e.g., systems, structures, components) of the same.
- alloy ingots are prepared by melting mixtures of good purity elements in an arc furnace or induction furnace.
- an arc furnace or induction furnace In order to produce homogeneous ingots of the complex alloys that contained manganese, refractory metals, and metalloids particularly carbon, it was found necessary to perform the alloying in two separate stages (or more).
- a mixture of all the elemental components except manganese was first melted together in an arc furnace. The ingot obtained was then combined with manganese and melted together to form the final ingot.
- stage 2 alloying it was found preferable to use clean manganese obtained by first pre-melting manganese pieces in an arc furnace.
- iron granules, graphite powders (about ⁇ 200 mesh), and molybdenum powders (about ⁇ 200 to ⁇ 375 mesh) plus chromium, boron, and phosphorous pieces were mixed well together and pressed into a disk or cylinder or any given mass.
- small graphite pieces in the place of graphite powders can also be used.
- the mass is melted in an arc furnace or induction furnace to form an ingot.
- the ingot obtained was then combined with manganese and melted together to form the final ingot.
- bulk-solidifying samples can be obtained using a conventional copper mold casting, for example, or other suitable methods.
- a conventional copper mold casting for example, or other suitable methods.
- DTA Differential Thermal Analyzer
- the present invention amorphous steel alloys were cast into cylinder-shaped amorphous rods with diameters reaching about 4 millimeter (mm).
- Various ranges of thickness, size, length, and volume are possible.
- the present invention alloys are processable into bulk amorphous samples with a range thickness of about 0.1 mm or greater.
- the amorphous nature of the rods is confirmed by x-ray and electron diffraction as well as thermal analysis (as shown in FIGS. 1 , 2 , and 3 ).
- the utilization of high-pressure casting methods and/or other emphasized methods produce thicker samples, including thick plates or as desired.
- the present alloys may be devitrified to form amorphous-crystalline microstructures, or blended with other ductile phases during solidification of the amorphous alloys to form composite materials, which can result in strong hard products with improved ductility for structural applications.
- the present invention amorphous steel alloys outperform current steel alloys in many application areas.
- Some products and services of which the present invention can be implemented includes, but is not limited thereto 1) ship, submarine (e.g., watercrafts), and vehicle (land-craft and aircraft) frames and parts, 2) building structures, 3) armor penetrators, armor penetrating projectiles or kinetic energy projectiles, 4) protection armors, armor composites, or laminate armor, 5) engineering, construction, and medical materials and tools and devices, 6) corrosion and wear-resistant coatings, 7) cell phone and personal digital assistant (PDA) casings, housings and components, 8) electronics and computer casings, housings, and components, 9) magnetic levitation rails and propulsion system, 10) cable armor, 11) hybrid hull of ships, wherein “metallic” portions of the hull could be replaced with steel having a hardened non-magnetic coating according to the present invention, 12) composite power shaft, 13) actuators and other utilization that require the combination of specific properties realiza
- two classes of non-ferromagnetic ferrous-based bulk amorphous metal alloys are obtained.
- the alloys in the subject two classes contain about 50 atomic % of iron.
- a high-manganese class (labeled MnB) contains manganese and boron as the principal alloying components.
- a high manganese-high molybdenum class (labeled MnMoC) contains manganese, molybdenum, and carbon as the principal alloying components.
- MnB high-manganese class
- MnMoC high manganese-high molybdenum class
- more than fifty compositions of each of the two classes are selected for testing glass formability.
- the MnB-class amorphous steel alloys are given by the formula (in atomic percent) as follows: (Fe 1-a-b-c Mn a Cr b Mo c ) 100-x-y-z Zr x Nb y B z where0.29 ⁇ a ⁇ 0.2, 0.1 ⁇ b ⁇ 0, 0.05 ⁇ c ⁇ 0, 10 ⁇ x ⁇ 2, 6 ⁇ y ⁇ 0, 24 ⁇ z ⁇ 13.
- the effectiveness in heat removal is significantly reduced, which limits the diameter of the amorphous rods to only about 2 mm in this embodiment.
- Various ranges of thickness are possible.
- the present invention alloys are processable into bulk amorphous samples with a range thickness of about 0.1 mm or higher.
- high-pressure squeeze casting exploits the full potential of these alloys as processable amorphous high-manganese steel alloys.
- Several atomic percent of carbon and/or silicon have also been substituted for boron in the above alloys.
- Nickel has also been used to partially substitute iron.
- the substituted alloys also exhibit T rg of about 0.6 and large supercooled liquid region of at least about 60° C.
- Table 1 summarizes results obtained from DTA scan of high-manganese (MnB) amorphous steel alloys of one exemplary embodiment. These exemplary embodiments are set forth for the purpose of illustration only and are not intended in any way to limit the practice of the invention.
- FIG. 4 shows the potentiodynamic polarization trace obtained on one of these alloys immersed in 0.6M NaCl pH:6.001 solution. The low passivating current, large passive region, and high pitting potential are noted.
- the composition region of these alloys can be given by the formula (in atomic percent) as follows: (Fe, Ni) a (Mn, Cr, Mo, Zr, Nb) b (B, Si, C) c where, 43 ⁇ a ⁇ 50, 28 ⁇ b ⁇ 36, 18 ⁇ c ⁇ 25, and the sum of a, b, and c is 100 and under the following constraints that Fe content is at least about 40%, Mn content is at least about 13%, Zr content is at least about 3%, and B content is at least about 12% in the overall alloy composition.
- These alloys are typically non-ferromagnetic and have low critical cooling rates of less than about 1,000° C./sec and castable into bulk objects of minimum dimension of at least about 0.5/mm. These alloys also have high T rg of about 0.60 or higher, and high ⁇ T x of about 50° C. or greater.
- the MnMoC-class amorphous steel alloys are given by the formula (in atomic percent) as follows: Fe 100-a-b-c-d-e Mn a Mo b Cr c B d C e where 13 ⁇ a ⁇ 8, 17 ⁇ b ⁇ 12, 5 ⁇ c ⁇ 0, 7 ⁇ d ⁇ 4, 17 ⁇ e ⁇ 13.
- alloys are found to exhibit a glass temperature T g of about 530-550° C. (or greater), T rg ⁇ 0.59-0.61 (or greater) and supercooled liquid region ⁇ T x of about 45-55° C. (or greater). DTA scans obtained from typical samples are shown in FIG. 3 .
- Some alloys also contain one to three atomic percent of Ga, V, and W additions.
- Various ranges of thickness are possible.
- the present invention alloys are processable into bulk amorphous samples with a range thickness of about 0.1 mm or greater.
- the MnMoC alloys can be readily cast into about 4 mm-diameter rods.
- a camera photo of two injection-cast amorphous rods is displayed in FIG. 5 .
- the alloy melts are observed to be much less viscous than the MnB-alloy melts.
- thicker samples can be achieved.
- Table 2 A variety of embodiments representing a number of typical amorphous steel alloys of the MnMoC class together with the sample thickness are listed in Table 2.
- Table 2 lists representative high manganese-high molybdenum (MnMoC) amorphous steel alloys and the maximum diameter of the bulk-solidifying amorphous cylinder-shaped samples obtained. At present, it is found in one embodiment that alloys containing as low as about 19 atomic % combined (B,C) metalloid content can be bulk solidified into about 3 mm-diameter amorphous rods.
- MnMoC manganese-high molybdenum
- FIG. 6 shows a typical potentiodynamic polarization trace obtained on approximately 3 mm-diameter samples of amorphous Fe 52 Mn 10 Mo 14 Cr 4 B 6 C 14 immersed in 0.6M NaCl pH:6.001 solution. The low passivating current, large passive region, and high pitting potential are noted.
- the composition of these alloys are given by the formula (in atomic percent) as follows: (Fe) a (Mn, Cr, Mo) b (B, C) c where, 45 ⁇ a ⁇ 55, 23 ⁇ b ⁇ 33, 18 ⁇ c ⁇ 24, and the sum of a, b, and c is 100 and under the following constraints that Mo content is at least about 12%, Mn content is at least about 7%, Cr content is at least about 3%, C content is at least about 13%, and B content is at least about 4% in the overall alloy composition.
- These alloys are typically non-ferromagnetic and have low critical cooling rates of less than about 1,000° C./sec and castable into bulk objects of minimum dimension of at least about 0.5/mm. These alloys also have high Trg of about 0.60 or greater, and high ⁇ T x of about 50° C. or greater.
- phosphorus has also been incorporated into the MnMoC-alloys to modify the metalloid content, with the goal of further enhancing the corrosion resistance.
- Various ranges of thickness are possible.
- the present invention alloys are processable into bulk amorphous samples with a range thickness of about 0.1 mm or greater.
- bulk-solidified non-ferromagnetic amorphous samples of up to about 3 mm in diameter was be obtained.
- amorphous steel alloys are given by the formula (in atomic percent) as follows: (Fe) a (Mn, Cr, Mo) b (B, P, C) c where, 47 ⁇ a ⁇ 59, 20 ⁇ b ⁇ 32, 19 ⁇ c ⁇ 23, and the sum of a, b, and c is 100 and under the following constraints that Mo content is at least 7%, Mn content is at least about 4%, Cr content is at least about 3%, C content is at least about 3%, P content is at least about 4%, and B content is at least about 4% in the overall alloy composition.
- These alloys are typically non-ferromagnetic and have low critical cooling rates of less than about 1,000° C./sec and castable into bulk objects of minimum dimension of at least about 0.5/mm. These alloys also have high T rg of about 0.60 or greater, and high ⁇ T x of about 50° C. or greater.
- the present invention amorphous steel alloys with high manganese content and related method of using and manufacturing the same provide a variety of advantages.
- the present invention provides both the non-ferromagnetic properties at ambient temperature as well as useful mechanical attributes.
- Another advantage of the present invention is that it provides a new class of ferrous-based bulk-solidifying amorphous metal alloys for non-ferromagnetic structural applications.
- the present invention alloys exhibit magnetic transition temperatures below the ambient, mechanical strengths and hardness superior to conventional steel alloys, and good corrosion resistance.
- advantages of the present invention include specific strengths as high as, for example, 0.5 MPa/(Kg/m3) (or greater), which are the highest among bulk metallic glasses.
- Another advantage of the present invention is that it possesses thermal stability highest among bulk metallic glasses.
- Another advantage of the present invention is that it has a reduced chromium content compared to current candidate Naval steels, for example.
- Another advantage of the present invention includes significantly lower ownership cost (for example, lower priced goods and manufacturing costs) compared with current refractory bulk metallic glasses.
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Abstract
Description
(Fe1-a-b-cMnaCrbMoc)100-x-y-zZrxNbyBz
where0.29≧a≧0.2, 0.1≧b≧0, 0.05≧c≧0, 10≧x≧2, 6≧y≧0, 24≧z≧13.
TABLE 1 |
High-Manganese (MnB) Amorphous Steel Alloys |
(Fe70Mn20Cr10)68Zr7Nb3B22 | Tg = 595° C.; ΔTx = 75° C.; |
Trg = 0.61 | |
(Fe70Mn25Cr5)68Zr7Nb3B22 | Tg = 613° C.; ΔTx = 78° C.; |
Trg = 0.61 | |
(Fe70Mn26.5Cr5)68Zr10C3B19 | Tg= 580° C.; ΔTx = 70° C.; |
Trg = 0.60 | |
(Fe70Mn26.5Cr5)68Zr7Nb3B22 | Tg = 613° C.; ΔTx = 78° C.; |
Trg = 0.61 | |
(Fe70Mn26.5Cr5)70Zr6Nb2B22 | Tg = 607° C.; ΔTx = 78° C.; |
Trg = 0.62 | |
(Fe70Mn26.5Cr5)70Zr4Nb4B22 | Tg = 595° C.; ΔTx = 78° C.; |
Trg = 0.62 | |
(Fe65Mn26Cr5Mo4)70Zr4Nb4B22 | Tg = 571° C.; ΔTx = 59° C.; |
Trg = 0.60 | |
(Fe70Mn26.5Cr5)68Zr6Nb6B20 | Tg = 595° C.; ΔTx = 94° C.; |
Trg = 0.60 | |
(Fe70Mn26.5Cr5)68Zr6Nb2B24 | Tg = 591° C.; ΔTx = 78° C.; |
Trg = 0.61 | |
(Fe70Mn26.5Cr5)68Zr4Nb4B24 | Tg = 613° C.; ΔTx = 85° C.; |
Trg = 0.63 | |
(Fe70Mn26.5Cr5)68Zr5Nb3B24 | Tg = 602° C.; ΔTx = 90° C.; |
Trg = 0.62 | |
(Fe65Mn26Cr5Mo4)68Zr4Nb4B24 | Tg = 585° C.; ΔTx = 90° C.; |
Trg = 0.62 | |
(Fe66Mn29Mo5)68Zr4Nb4B24 | Tg = 605° C.; ΔTx = 87° C.; |
Trg = 0.63 | |
(Fe66Mn29Cr5)68Zr4Nb4B24 | Tg = 600° C.; ΔTx = 100° C.; |
Trg = 0.62 | |
(Fe70Mn26.5Cr5)68Zr4Ti4B24 | Tg = 560° C.; ΔTx = 60° C.; |
Trg = 0.59 | |
(Fe66Mn29Mo5)68Zr4Nb4B20Si4 | Tg~590° C.; ΔTx = 72° C.; Trg~0.63 |
(Fe66Mn29Mo5)68Zr4Nb4B22Si2 | Tg~595° C.; ΔTx = 75° C.; Trg~0.63 |
(Fe70Mn25Cr5)68Zr7Nb3C3B13Si6 | Tg = 573° C.; ΔTx = 90° C.; |
Trg = 0.60 | |
(Fe60Mn25Cr5Ni10)68Zr7Nb3B22 | Tg = 572° C.; ΔTx = 75° C.; |
Trg = 0.59 | |
(Fe70Mn26.5Cr5)68Zr10C3B19 | Tg = 580° C.; ΔTx = 72° C.; |
Trg = 0.60 | |
(Fe, Ni)a(Mn, Cr, Mo, Zr, Nb)b(B, Si, C)c
where, 43≧a≧50, 28≧b≧36, 18≧c≧25, and the sum of a, b, and c is 100 and under the following constraints that Fe content is at least about 40%, Mn content is at least about 13%, Zr content is at least about 3%, and B content is at least about 12% in the overall alloy composition. These alloys are typically non-ferromagnetic and have low critical cooling rates of less than about 1,000° C./sec and castable into bulk objects of minimum dimension of at least about 0.5/mm. These alloys also have high Trg of about 0.60 or higher, and high ΔTx of about 50° C. or greater.
Fe100-a-b-c-d-eMnaMobCrcBdCe
where 13≧a≧8, 17≧b≧12, 5≧c≧0, 7≧d≧4, 17≧e≧13.
TABLE 2 |
High Manganese-High Molybdenum (MnMoC) Amorphous Steel Alloys |
Fe54Mn10Mo14B7C15 | 3 mm | ||
Fe49Mn8Mo13Cr5W3B7C15 | 2 mm | ||
Fe49Mn10Mo14Cr4B7C16 | 2 mm | ||
Fe49Mn10Mo14Cr4Ga1B7C15 | 2 mm | ||
Fe46Mn10Mo16Cr4Ga2B7C15 | 2 mm | ||
Fe49Mn10Mo14Cr4V1B7C15 | 3 mm | ||
Fe49Mn10Mo14Cr4W1B7C15 | 3 mm | ||
Fe51Mn10Mo13Cr4B7C15 | 3 mm | ||
Fe51Mn10Mo14Cr4B6C15 | 4 mm | ||
Fe52Mn10Mo14Cr4B6C14 | 4 mm | ||
Fe49Mn10Mo14Cr4W1B6C16 | 4 mm | ||
Fe49Mn10Mo15Cr4B6C16 | 4 mm | ||
Fe52Mn10Mo14Cr4B5C15 | 3 mm | ||
Fe53Mn10Mo14Cr4B5.5C13.5 | 3 mm | ||
Fe50Mn10Mo14Cr4B5C17 | 3 mm | ||
Fe48Mn10Mo16Cr4B7C15 | 3 mm | ||
Fe50Mn10Mo14Cr4B7C15 | 3 mm | ||
Fe50Mn8Mo14Cr3W3B7C15 | 3 mm | ||
Fe48Mn10Mo13Cr4W3B7C15 | 2 mm | ||
Fe49Mn10Mo13Cr3W3B7C15 | 2 mm | ||
Fe47Mn10Mo18Cr3B7C15 | 2 mm | ||
Fe48Mn12Mo14Cr4C15B7 | 1.5 mm | ||
(Fe)a(Mn, Cr, Mo)b(B, C)c
where, 45≧a≧55, 23≧b≧33, 18≧c≧24, and the sum of a, b, and c is 100 and under the following constraints that Mo content is at least about 12%, Mn content is at least about 7%, Cr content is at least about 3%, C content is at least about 13%, and B content is at least about 4% in the overall alloy composition. These alloys are typically non-ferromagnetic and have low critical cooling rates of less than about 1,000° C./sec and castable into bulk objects of minimum dimension of at least about 0.5/mm. These alloys also have high Trg of about 0.60 or greater, and high ΔTx of about 50° C. or greater.
Fe100-a-b-c-d-e-fMnaMobCrcBdPeCf
where 15≧a≧5, 14≧b≧8, 10≧c≧4, 8≧d≧0, 12≧e≧5, 16≧f≧4.
Fe48Mn10Mo13Cr4W3C16P6 | 2 mm | ||
Fe52Mn10Cr4Mo14C4P12B4 | 2 mm | ||
Fe58Mn10Cr4Mo8C4P12B4 | 2 mm | ||
Fe52Mn10Cr6Mo12C4P12B4 | 2 mm | ||
Fe52Mn10Mo10Cr8C4P12B4 | 2 mm | ||
Fe53Mn10Mo12Cr4C7P7B7 | 3 mm | ||
Fe53Mn10Mo12Cr4C7P9B5 | 2 mm | ||
Fe58Mn5Cr4Mo12C7P7B7 | 2 mm | ||
Fe48Mn15Cr4Mo12C7P7B7 | 2 mm | ||
Fe48Mn10Cr4Mo12C8P5B8 | 1.5 mm | ||
(Fe)a(Mn, Cr, Mo)b(B, P, C)c
where, 47≧a≧59, 20≧b≧32, 19≧c≧23, and the sum of a, b, and c is 100 and under the following constraints that Mo content is at least 7%, Mn content is at least about 4%, Cr content is at least about 3%, C content is at least about 3%, P content is at least about 4%, and B content is at least about 4% in the overall alloy composition. These alloys are typically non-ferromagnetic and have low critical cooling rates of less than about 1,000° C./sec and castable into bulk objects of minimum dimension of at least about 0.5/mm. These alloys also have high Trg of about 0.60 or greater, and high ΔTx of about 50° C. or greater.
U.S. Pat. No. 5,738,733 | Inoue A. et al. | ||
U.S. Pat. No. 5,961,745 | Inoue A. et al. | ||
U.S. Pat. No. 5,976,274 | Inoue A. et al. | ||
U.S. Pat. No. 6,172,589 | Fujita K. et al. | ||
U.S. Pat. No. 6,280,536 | Inoue A. et al. | ||
U.S. Pat. No. 6,284,061 | Inoue A. et al. | ||
U.S. Pat. No. 5,626,691 | Li, Poon, and Shiflet | ||
U.S. Pat. No. 6,057,766 | O'Handley et al. | ||
-
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Claims (22)
Fe100-a-b-c-d-eMnaMobCrcBdCe
ΔT x =T x −T g
Trg=Tg/Tl
Fe100-a-b-c-d-eMnaMobCrcBdCe
(Fe)a(Mn, Cr, Mo)b(B, C)c
(Fe)a(Mn, Cr, Mo)b(B, C)c
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AU2003216234A8 (en) | 2003-09-04 |
AU2003216234A1 (en) | 2003-09-04 |
WO2003069000A3 (en) | 2003-12-24 |
JP2005517808A (en) | 2005-06-16 |
US20060283527A1 (en) | 2006-12-21 |
EP1485512A4 (en) | 2005-08-31 |
US20030164209A1 (en) | 2003-09-04 |
WO2003069000A2 (en) | 2003-08-21 |
CN1646718A (en) | 2005-07-27 |
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KR20040081784A (en) | 2004-09-22 |
US7067020B2 (en) | 2006-06-27 |
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